chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	2711603	2711604	G	C	5	GENIC	homozygous	113498862
4	2712714	2712715	A	G	22	GENIC	homozygous	113498865
4	2717274	2717275	C	T	34	GENIC	homozygous	113498867
4	2717845	2717846	T	C	26	GENIC	homozygous	112465589
4	2723126	2723127	G	T	28	GENIC	homozygous	112465597
4	2723644	2723645	T	C	33	GENIC	homozygous	112465599
4	2723938	2723939	C	T	22	GENIC	heterozygous	119334115
4	2726977	2726978	T	C	31	GENIC	homozygous	112465601
4	2730682	2730683	C	T	36	GENIC	homozygous	112465605
4	2735653	2735654	A	T	20	GENIC	homozygous	112465611
4	2740250	2740251	A	G	59	GENIC	heterozygous	112465631
4	2740545	2740546	T	C	65	GENIC	heterozygous	112465637
4	2740546	2740547	G	A	66	GENIC	heterozygous	112465639
4	2740569	2740570	T	C	77	GENIC	heterozygous	113229094
4	2740646	2740647	G	A	57	GENIC	heterozygous	112465641
4	2740667	2740668	A	G	49	GENIC	heterozygous	112465643
4	2740722	2740723	A	C	53	GENIC	heterozygous	112465645
4	2740736	2740737	T	A	51	GENIC	heterozygous	112465649
4	2740767	2740768	C	T	55	GENIC	heterozygous	113229095
4	2740788	2740789	A	G	65	GENIC	heterozygous	112995714
4	2753551	2753552	A	G	28	GENIC	homozygous	112995724
4	2753552	2753553	G	A	28	GENIC	homozygous	113073697
4	2754440	2754441	A	G	17	GENIC	homozygous	112465677
4	2754710	2754711	A	G	23	GENIC	homozygous	112465679
4	2756943	2756944	T	C	27	GENIC	homozygous	113498874
4	2771783	2771784	T	G	32	GENIC	homozygous	112465701